Polypyrrole (PPy) conducting films, doped with 4-amino-3-hydroxynaphthalene sulfonic acid (AHNSA), were electrosynthesized by anodic oxidation of pyrrole on Pt and steel electrodes in aqueous medium (0.01 M AHNSA +0.007 M NaOH, using cyclic voltammetry (CV), and their electrochemical properties were studied. Fourier-transform infrared (FT-IR) spectroscopy confirmed the formation of AHNSA-PPy films. Their morphology was characterized by scanning electron microscopy (SEM), and their optical properties, including UV-VIS absorption and fluorescence spectra, were also investigated. AHNSA-PPy films were used for the removal of chromium(VI) from aqueous solution, by means of the immersion method and the Cr(VI) electro-reduction method. The effect of various experimental parameters, including the adsorbent (polymer) mass, pH, type of electrodes, and current intensity, on the adsorption of chromium by the polymer was performed and optimized. The adsorption and electro-reduction of (Cr VI) on the AHNSA-PPy film surface were found to be highly pH-dependent, and the kinetics of Cr(VI) adsorption and electro-reduction followed second-order kinetic curves. Apparent second-order rate constants were about three times higher for the Cr(VI) electro-reduction method than for the immersion method, indicating that the use of electro-reduction method significantly accelerated the chromium adsorption process on polymer. The maximum adsorption capacity of the AHNSA-PPy film for chromium was 224 mg g. A 96% chromium removal from pure aqueous solution was reached within about 48 h by the immersion method, but only within about 6 h by the Cr(VI) electro-reduction method. Application of both methods to Cr(VI) fortified natural waters of Senegal led to chromium removal efficiency high values (93 to 96% according to the type of natural water).
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http://dx.doi.org/10.1007/s11356-017-9713-y | DOI Listing |
Inorg Chem
December 2024
Department of Chemistry, University of Kansas, 1567 Irving Hill Road, Lawrence, Kansas 66045, United States.
Interconversion of the oxidation states of uranium enables separations and reactivity schemes involving this element and contributes to technologies for recycling of spent nuclear fuels. The redox behaviors of uranium species impact these processes, but use of electrochemical methods to drive reactions of molecular uranium complexes and to obtain molecular insights into the outcomes of electrode-driven reactions has received far less attention than it deserves. Here, we show that electro-reduction of the uranyl ion (UO) can be used to promote stepwise functionalization of the typically unreactive oxo groups with exogenous triphenylborane (BPh) serving as a moderate electrophile, avoiding the conventional requirement for a chemical reductant.
View Article and Find Full Text PDFNanotechnology
December 2024
Zhejiang University of Technology, No. 18 Chaowang Road, Hangzhou, 310014, CHINA.
Electrocatalytic nitrogen reduction reaction (NRR) is a prospective tactics for ammonia synthesis. However, the development of highly active NRR electrocatalysts is still challenging owing to the difficult activation of nitrogen and competitive hydrogen evolution reaction (HER). Here, we synthesized boron-doped AuRh mesoporous nanotubes (B-AuRh MNTs) via dual-template method coupled with boron doping.
View Article and Find Full Text PDFSmall Methods
December 2024
Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Jiangsu Province Key Laboratory of Green Biomass-based Fuels and Chemicals, College of Chemical Engineering, Nanjing Forestry University, Nanjing, Jiangsu, 210037, China.
This work reports boron and oxygen dual-doped carbon nitride nanotubes (B/O-CNNTs) prepared via a copolymerization process for electrocatalytic ammonia synthesis from nitrogen gas (NRR) and nitrate (NORR) sources, respectively. By adjusting the dosage of boron oxide precursor, the texture and content of B/O dual dopants and the coordination environment in the resulting 1D CNNTs can be tuned. The best B/O-CNNTs can achieve maximum Faradaic efficiencies of 35% and 96% at -1.
View Article and Find Full Text PDFJ Am Chem Soc
September 2024
Department of Chemistry, Purdue University, West Lafayette, Indiana 47907, United States.
We have discovered a strategy to synthesize reactive radical salts, effectively bottling up radicals in space and time for future use. We apply this new principle to electrochemiluminescence (ECL) through the simultaneous electro-reduction of peroxydisulfate, SO, and tris(bipyridine)ruthenium(II), [Ru(bpy)] in a water/acetonitrile mixture. The electrode generates a concentration profile exceeding the solubility of the cation and anion pair, promoting precipitation.
View Article and Find Full Text PDFEnviron Res
November 2024
Well Fore Special Wire Corporation, 10, Tzu-Chiang 7th., Chung-Li Industrial Park, Taoyuan, Taiwan.
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